插层(化学)
双层
材料科学
锂(药物)
相(物质)
拉曼光谱
化学物理
结晶学
相变
兴奋剂
纳米技术
凝聚态物理
化学
无机化学
光电子学
光学
内分泌学
物理
医学
有机化学
生物化学
膜
作者
Yecun Wu,Jingyang Wang,Yanbin Li,Jiawei Zhou,Bai Yang Wang,Ankun Yang,Lin‐Wang Wang,Harold Y. Hwang,Yi Cui
标识
DOI:10.1038/s41467-022-30516-z
摘要
Lithium intercalation of MoS2 is generally believed to introduce a phase transition from H phase (semiconducting) to T phase (metallic). However, during the intercalation process, a spatially sharp boundary is usually formed between the fully intercalated T phase MoS2 and non-intercalated H phase MoS2. The intermediate state, i.e., lightly intercalated H phase MoS2 without a phase transition, is difficult to investigate by optical-microscope-based spectroscopy due to the narrow size. Here, we report the stabilization of the intermediate state across the whole flake of twisted bilayer MoS2. The twisted bilayer system allows the lithium to intercalate from the top surface and enables fast Li-ion diffusion by the reduced interlayer interaction. The E2g Raman mode of the intermediate state shows a peak splitting behavior. Our simulation results indicate that the intermediate state is stabilized by lithium-induced symmetry breaking of the H phase MoS2. Our results provide an insight into the non-uniform intercalation during battery charging and discharging, and also open a new opportunity to modulate the properties of twisted 2D systems with guest species doping in the Moiré structures.
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